HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → HCID 23447770, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | Phenylthiourea | HCID 676454 | — |
| Reactant | HCID 23447739 | HCID 23447739 | — |
| Product | HCID 23447770 | HCID 23447770 | 57.4% |
Reaction Steps
Following the general procedure for protected phenyl thiourea formation outlined in example 12, N-[4-Chloro-2-hydroxy-3-[N″,N″-dimethylaminosulfonyl]phenyl]-N′-(2-methylphenyl)thiourea (557 mg, 1.39 mmol), tert-butyldimethylsilyl chloride (1.04 mg, 6.95 mmol) and imidazole (189 mg, 2.78 mmol) were reacted to form the desired product (410 mg, 57%). EI-MS m/z 514.2 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06680317B2 |
| Source dataset | uspto-grants-2004_01 |
| ORD ID | ord-a35529c533694e7ca217ac4ceabeaa94 |
| Source note | uspto-grants-2004_01 |